Assistant Clinical Research Manager - Regional Campuses

The Assistant Clinical Research Manager (ACRM) supports clinical research programs and teams across Dana-Farber’s regional satellite locations. Working under the direction of Principal Investigators and in collaboration with Clinical Research Managers, physicians, and research nursing staff, the ACRM helps oversee the conduct of clinical trials in accordance with Good Clinical Practice. Key responsibilities include supporting the design, implementation, and evaluation of clinical research activities; assisting with regulatory oversight; and providing day-to-day supervision of clinical research staff as needed.

This position requires weekly travel and onsite work at various regional campuses, with the ability to work remotely up to one day per week. Remote work must be performed from a New England state (ME, VT, NH, MA, CT, or RI). Dana-Farber’s regional locations include Attleboro, Boston, Brookline, Brighton, Foxborough, Milford, Methuen, and Weymouth, Massachusetts, as well as Londonderry, New Hampshire.

Located in Boston and the surrounding communities, Dana-Farber Cancer Institute is a leader in life changing breakthroughs in cancer research and patient care. We are united in our mission of conquering cancer, HIV/AIDS, and related diseases. We strive to create an inclusive, diverse, and equitable environment where we provide compassionate and comprehensive care to patients of all backgrounds, and design programs to promote public health particularly among high-risk and underserved populations. We conduct groundbreaking research that advances treatment, we educate tomorrow's physician/researchers, and we work with amazing partners, including other Harvard Medical School-affiliated hospitals.

ROLE & RESPONSIBILITIES:

Clinical Trials Operations

• Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group’s clinical trial portfolio and all related regulatory and compliance requirements.
• The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group’s portfolio. They will be responsible for the required tracking of all protocol development, submission, review and approval milestones.
• The ACRM will assist with the oversight of subject enrollment, protocol treatment and follow-up care processes for protocol patients.
• Assist with the oversight of registration of protocol patients, study group registrar and pharmaceutical company as outlined in protocol.

Regulatory & Compliance

• Assists in the responsibility for essential document compliance for entire portfolio. Implements systems to monitor and ensure regulatory document collection and maintenance compliance.
• Assists in the responsibilities for all clinical trial reporting requirements; safety event, annual approval, deviations etc. May implement systems to monitor portfolio compliance.
• Assists the study team to be maintain an “audit ready” research environment

Data Management & Clinical Trial Monitoring

• Assists CRM with responsibility for data management and compliance for entire portfolio. Maintains schedules and procedures necessary for timely and complete data collection.
• Regularly reports data compliance status to key stakeholders; i.e. DFCI PI, study Sponsor, DFCI CTO. Helps to implement corrective action to maintain data compliance when necessary.
• Submits required “progress / tracking “reports to key stakeholders, when applicable.

Staff Training & Development

• Will assist the CRM with the recruitment and oversight of coordinator staff as well as ensures that staff have completed mandatory training in a timely manner.
• Will help implement program specific on-boarding and orientation process and may participate in annual performance evaluations and competency assessments of research staff as needed.

KNOWLEDGE, SKILLS, AND ABILITIES REQUIRED

• Must be able to perform day-to-day responsibilities independently with minimal supervision from managers.
• Has the ability to identify regulatory scenarios that require consultation.
• Has a good understanding of clinical trials start-up, active and close out phases.
• Has a good understanding of clinical research, local policy and federal regulation.
• Knowledge of cancer as a disease process, cancer treatment modalities, and the clinical trial process.
• In addition, has experience in protocol development, data compilation and analysis.
• The ACRM will have a good understanding of the various tracking systems used to ensure timely data management by the clinical research staff.
• They will also understand Federal and State regulations as they relate to research. Strong interpersonal, organizational and communication skills are required.
• Must have computer skills including the use of Microsoft Office.

MINIMUM JOB QUALIFICATIONS

• Bachelor’s Degree required.
• Minimum of 3 plus years of related experience preferred.
• Must have the ability to function independently, think critically and with good professional judgment.

SUPERVISORY RESPONSIBILITIES

• No direct reports.
• Will provide day to day supervision for study management staff, including clinical research coordinators, students, volunteers, and other research assistants as needed.

PATIENT CONTACT

• May have contact with patients of all ages and populations.

At Dana-Farber Cancer Institute, we work every day to create an innovative, caring, and inclusive environment where every patient, family, and staff member feels they belong. As relentless as we are in our mission to reduce the burden of cancer for all, we are committed to having faculty and staff who offer multifaceted experiences. Cancer knows no boundaries and when it comes to hiring the most dedicated and compassionate professionals, neither do we. If working in this kind of organization inspires you, we encourage you to apply.

Dana-Farber Cancer Institute is an equal opportunity employer and affirms the right of every qualified applicant to receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, national origin, sexual orientation, genetic information, disability, age, ancestry, military service, protected veteran status, or other characteristics protected by law.

EEO Poster

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Pay Transparency Statement

The hiring range is based on market pay structures, with individual salaries determined by factors such as business needs, market conditions, internal equity, and based on the candidate’s relevant experience, skills and qualifications.

For union positions, the pay range is determined by the Collective Bargaining Agreement (CBA).

$70,000.00 - $85,300.00